Advanced Search
YANG Meiling, LI Jing, LI Zhiqiang, ZHONG Yu, WANG Yan, LI Zhong, HOU Youxian, JIA Junsong, CHEN Jing. Acute Haematological Toxicity for Patients Treated with Craniospinal Irradiation Helical Tomotherapy Versus Conventional Radiotherapy[J]. Cancer Research on Prevention and Treatment, 2014, 41(11): 1215-1218. DOI: 10.3971/j.issn.1000-8578.2014.11.012
Citation: YANG Meiling, LI Jing, LI Zhiqiang, ZHONG Yu, WANG Yan, LI Zhong, HOU Youxian, JIA Junsong, CHEN Jing. Acute Haematological Toxicity for Patients Treated with Craniospinal Irradiation Helical Tomotherapy Versus Conventional Radiotherapy[J]. Cancer Research on Prevention and Treatment, 2014, 41(11): 1215-1218. DOI: 10.3971/j.issn.1000-8578.2014.11.012

Acute Haematological Toxicity for Patients Treated with Craniospinal Irradiation Helical Tomotherapy Versus Conventional Radiotherapy

More Information
  • Received Date: September 17, 2013
  • Revised Date: November 28, 2013
  • Objective To compare the acute haematological toxicity for patients treated with craniospinal irradiation (CSI) using helical tomotherapy (HT) and conventional radiotherapy (CRT). Methods We retrospectively analyzed the acute haematology data of 70 hospitalized patients treated with CSI. Patients were divided into helical tomotherapy group (HT, 14 cases) and conventional radiotherapy group(CRT, 56 cases). Myelosuppression of two groups were recorded and compared according to CTCAE v3.0. Difference was compared by χ2 test. Results The incidence of leucopenia, thrombocytopenia and decreased hemoglobin were 100%, 100%, 78.6% in HT group and 91.1%, 67.9%,32.1% in CRT group, respectively(P<0.05); moreover, the incidence at grade Ⅲ-Ⅳ were 85.7%, 50%, 14.2% in HT group and 35.8%, 10.7%, 0 in CRT group, respectively(P<0.05). There were 10.7%(6/56) patients in CRT group and 92.8%(10/14)patients in HT group were delayed radiotherapy due to myelosuppression (P<0.05). The average myelosuppression time was 11.5 d in HT group and 17.37 d in CRT group (P<0.05).Myelosuppression was more serious in patients treated with induction chemotherapy than those without induction chemotherapy before radiotherapy. Conclusion HT shows more serious hematologic toxicity compared with CRT, which may relate to low dose exposure range for bone marrow and whole body, chemotherapy, etc. More attention and researches should be applied to the acute haematological toxicity of HT.
  • [1]
    Li J, Li ZQ, Wen T, et al. Observation of acute toxicity of craniospinal irradiation by helical tomotherapy[J]. Zhongguo Wei Qin Xi Shen Jing Wai Ke Za Zhi, 2013, 18(2):72-4. [黎静, 李志强, 文婷, 等. 螺旋断层放疗技术进行全中枢照射急性毒副反应的 初步观察[J]. 中国微侵袭神经外科杂志, 2013, 18(2):72-4.]
    [2]
    Paulino AC, Wen BC, Mayr NA,et al. Protracted radiotherapy treatment duration in medulloblastoma[J].Am J Clin Oncol, 2003, 26 (1):55-9.
    [3]
    Jeffries S, Rajan B, Ashely S, et al. Haematological toxicity of cranio-spinal irradiation[J]. Radiother Oncol, 1998, 48(1):23-7.
    [4]
    Sugie C, Shibamoto Y, Ayakawa S, et al. Craniospinal irradiation using helical tomotherapy: evaluation of acute toxicity and dose distribution[J]. Technol Cancer Res Treat, 2011, 10(2): 187-95.
    [5]
    Mesbah L, Matute R, Usychkin S, et al. Helical tomotherapy in the treatment of pediatric malignancies: a preliminary report of feasibility and acute toxicity[J]. Radiat Oncol, 2011, 6:102.
    [6]
    Lopez Guerra JL, Marrone I, Jaen J, et al. Outcome and toxicity using helical tomotherapy for craniospinal irradiation in pediatric medulloblastoma[J]. Clin Transl Oncol, 2014, 16(1): 96-101.
    [7]
    Peñagarícano JA, Papanikolaou N, Yan Y, et al. Feasibility of cranio-spinal axis radiation with the Hi-Art tomotherapy system[J]. Radiother Oncol, 2005, 76(1):72-8.
    [8]
    Lee IJ, Seong J, Lee CG, et al. Early clinical experience and outcome of helical tomotherapy for multiple metastatic lesions[J]. Int J Radiat Oncol Biol Phys, 2009, 73(5):1517-24.
    [9]
    Wen T, LI ZQ, Zhang JJ, et al. Craniospinal irradiation using improved helical tomotherapy: evaluation of clinical feasibility[J]. Zhongguo Yi Xue Wu Li Xue Za Zhi, 2012, 29(6):3737-41.[文婷, 李志强, 张晋建,等.改进全脑全脊髓螺旋断层放射治疗计划的 研究[J] 中国医学物理学杂志, 2012, 29(6):3737-41.]
    [10]
    Mac Manus M, Lamborn K, Khan W, et al. Radiotherapyassociated neutropenia and thrombocytopenia: analysis of risk factors and development of a predictive model[J]. Blood, 1997, 89 (7):2303-10.
    [11]
    Chang EL, Allen P, Wu C, et al. Acute toxicity and treatment interruption related to electron and photon craniospinal irradiation in pediatric patients treated at the University of Texas M. D. Anderson Cancer Center[J].Int J Radiat Oncol Biol Phys, 2002, 52 (4):1008-16.
  • Related Articles

    [1]LU Xin, KONG Lingyu, JIA Lei, JIANG Lingling. Mechanism of D-bifunctional Protein Promoting Formation of Hepatocellular Carcinoma in Rat via STAT3[J]. Cancer Research on Prevention and Treatment, 2019, 46(8): 690-695. DOI: 10.3971/j.issn.1000-8578.2019.19.0170
    [2]Cui Na, Chen Zhi, Li Xiaolei, Dong Xumei, Zhang Luhua, Li Na′na, Wang Yaqing. Experimental Intervention of Phytoestrogens on Breast Cancer Development in Young Female SD Rats[J]. Cancer Research on Prevention and Treatment, 2012, 39(07): 773-775. DOI: 10.3971/j.issn.1000-8578.2012.07.003
    [3]Wang Jiyun, Zhang Junquan, Zhang Jianwei, Wang Jianjun, Liu Bengang, Li Wangang. Effects of Chronic Composite Stress on Cell Immunity and Tumor Marker in Esophageal Neoplasia Model Rats[J]. Cancer Research on Prevention and Treatment, 2012, 39(01): 28-31. DOI: 10.3971/j.issn.1000-8578.2012.01.007
    [4]DONG Lin, GE Rui-min, QI Nan, SHEN Li. JNK1 Knockdown via Adenovirus-mediated shRNA Inhibited Cell Proliferation in U87MG Gliobalstoma Cells[J]. Cancer Research on Prevention and Treatment, 2011, 38(07): 767-769. DOI: 10.3971/j.issn.1000-8578.2011.07.010
    [5]WU Zhi-ping, GAO Cheng-wei, WU Yong-gui, ZHU Qi-shun, WANG Xi-cai, LIU Xin, LIU Chuen, TONG Shu-yun. Inhibitive Effect of Artemether on Glioma Growth in SD Rat Orthotopic Glioma Model[J]. Cancer Research on Prevention and Treatment, 2010, 37(06): 614-616. DOI: 10.3971/j.issn.1000-8578.2010.06.002
    [6]WU Zhi-ping, GAO Cheng-wei, WU Yong-gui, ZHU Qi-shun, WANG Xi-cai, LIU Xin, LIU Chun. Inhibitive Effect of Artemether on Brain Glioma Angiogenesis in SD Rat[J]. Cancer Research on Prevention and Treatment, 2009, 36(03): 186-189. DOI: 10.3971/j.issn.1000-8578.2009.03.005
    [7]GUAN Jian, CHEN Long-hua, LI Zhi-yong, LI Qi-sheng, LIU Ying, WANG Hong-mei. Rat Model Establ ishment of Brain Radiation Injury[J]. Cancer Research on Prevention and Treatment, 2007, 34(07): 477-479. DOI: 10.3971/j.issn.1000-8578.1268
    [8]HAN Dan, ZHAO Chuan, JING Shu-zhen. Pathological Change in the Experimental Rat s MPM[J]. Cancer Research on Prevention and Treatment, 2006, 33(10): 743-745. DOI: 10.3971/j.issn.1000-8578.868
    [9]LIU Hong-yao, LIU Chun, MI Zheng-guo, et al, . Expermental Model of Bladder Tumors in Rats In duced by MNU[J]. Cancer Research on Prevention and Treatment, 2000, 27(04): 241-243. DOI: 10.3971/j.issn.1000-8578.780
    [10]Wu Wensen, . The Effect of Female hormones in stopping growth of MNU-induced Urinary bladder tumors in Rats and reducing the size of tumors in Mice[J]. Cancer Research on Prevention and Treatment, 1996, 23(1): 4-7.

Catalog

    Article views (1397) PDF downloads (433) Cited by()

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return